review article | Q7318358 |
case report | Q2782326 |
scholarly article | Q13442814 |
P2093 | author name string | Jie Li | |
Qian Zhang | |||
Jian Zhu | |||
Yi-Ming Mu | |||
Shi-Hui Wei | |||
Wei-Jun Gu | |||
P2860 | cites work | The prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and/or central diabetes insipidus and review of the literature | Q26866028 |
International Consensus Guidance Statement on the Management and Treatment of IgG4-Related Disease | Q27970302 | ||
Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapy | Q30651194 | ||
Prednisolone markedly reduced serum IgG4 levels along with the improvement of pituitary mass and anterior pituitary function in a patient with IgG4-related infundibulo-hypophysitis | Q30714403 | ||
Occurrence of IgG4-related hypophysitis lacking IgG4-bearing plasma cell infiltration during steroid therapy | Q30791963 | ||
A case of suspected lymphocytic hypophysitis and organizing pneumonia during maintenance therapy for autoimmune pancreatitis associated with autoimmune thrombocytopenia | Q33371988 | ||
Long-term clinical course of IgG4-related systemic disease accompanied by hypophysitis | Q33550042 | ||
Histologically confirmed isolated IgG4-related hypophysitis: two case reports in young women. | Q34241475 | ||
IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. | Q35101828 | ||
Clinical course of IgG4-related hypophysitis presenting with focal seizure and relapsing lymphocytic hypophysitis | Q35824920 | ||
Autoimmune hypophysitis. | Q36000933 | ||
Hypophysitis presented as inflammatory pseudotumor in immunoglobulin G4-related systemic disease | Q36978379 | ||
Optimising corticosteroid treatment for autoimmune pancreatitis | Q36999326 | ||
IgG4-related sclerosing disease: a critical appraisal of an evolving clinicopathologic entity | Q37781971 | ||
IgG4-related systemic disease in a Native American man. | Q37866008 | ||
A case of IgG4-related hypophysitis without pituitary insufficiency | Q38091622 | ||
Clinical features of 10 patients with IgG4-related retroperitoneal fibrosis | Q38121780 | ||
Inflammatory pseudotumors in multiple organs associated with elevated serum IgG4 level: recovery by only a small replacement dose of steroid | Q40416847 | ||
IgG4-associated multifocal systemic fibrosis complicating sclerosing sialadenitis, hypophysitis, and retroperitoneal fibrosis, but lacking pancreatic involvement. | Q40463357 | ||
Thickened Pituitary Stalk Associated with a Mass in the Sphenoidal Sinus: An Alarm to Suspect Hypophysitis by Immunoglobulin G4? | Q41443579 | ||
IgG4-Related Disease without Overexpression of IgG4: Pathogenesis Implications | Q42278748 | ||
A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus | Q42906513 | ||
Putative IgG4-related pituitary disease with hypopituitarism and/or diabetes insipidus accompanied with elevated serum levels of IgG4. | Q43064024 | ||
Treatment of relapsing autoimmune pancreatitis with immunomodulators and rituximab: the Mayo Clinic experience | Q43472409 | ||
Standard steroid treatment for autoimmune pancreatitis. | Q46034514 | ||
A case of IgG4-related multifocal fibrosclerosis complicated by central diabetes insipidus | Q46584974 | ||
IgG4-related hypophysitis presenting as a pituitary adenoma with systemic disease | Q48113939 | ||
Hypophysitis presenting with atypical rapid deterioration: with special reference to immunoglobulin G4-related disease-case report-. | Q48368362 | ||
A case of Mikulicz's disease (IgG4-related plasmacytic disease) complicated by autoimmune hypophysitis | Q48388498 | ||
[Two cases of IgG4-related systemic disease arising from urinary tract]. | Q50498642 | ||
[Clinicopathological features of neuropathy associated with IgG4-related disease]. | Q53620006 | ||
Amendment of the Japanese Consensus Guidelines for Autoimmune Pancreatitis, 2013 III. Treatment and prognosis of autoimmune pancreatitis | Q60609861 | ||
High serum IgG4 concentrations in patients with sclerosing pancreatitis | Q73583110 | ||
Autoimmune pancreatitis | Q80147141 | ||
Multiple pseudotumors in IgG4-associated multifocal systemic fibrosis | Q81104496 | ||
Serial changes of elevated serum IgG4 levels in IgG4-related systemic disease | Q83232220 | ||
[A case of IgG4-related disease with deterioration in pulmonary and pituitary involvements during a 10-year clinical course of inflammatory pseudotumor] | Q83480097 | ||
[Case report: IgG4-related hypophysitis presenting with secondary adrenal insufficiency and central diabetes insipidus in a type 1 diabetes patient] | Q84232115 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International | Q24082749 |
P433 | issue | 24 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | globulins | Q321710 |
rituximab | Q412323 | ||
monoclonal antibody | Q422248 | ||
blood proteins | Q425056 | ||
eye disease | Q3041498 | ||
immunologic factor | Q50349184 | ||
murine-derived monoclonal antibodies | Q68944048 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | e6934 | |
P577 | publication date | 2017-06-01 | |
P1433 | published in | Medicine | Q15716652 |
P1476 | title | Rituximab was used to treat recurrent IgG4-related hypophysitis with ophthalmopathy as the initial presentation: A case report and literature review | |
P478 | volume | 96 |
Q47296234 | A case series of atypical features of patients with biopsy-proven isolated IgG4-related hypophysitis and normal serum IgG4 levels |
Q92591462 | Clinical Characteristics of 76 Patients with IgG4-Related Hypophysitis: A Systematic Literature Review |
Q64039689 | Disease heterogeneity in IgG4-related hypophysitis: report of two histopathologically proven cases and review of the literature |
Q89310972 | Sustained clinical response after single course of rituximab as first-line monotherapy in adult-onset asthma and periocular xanthogranulomas syndrome associated with IgG4-related disease: A case report |
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